DYRK1A-related intellectual disability syndrome
MONDO:0013578An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYRK1A on chromosome 21q22.13.
Also known as: MRD7, autosomal dominant intellectual disability 7, intellectual disability, autosomal dominant type 7, mental retardation, autosomal dominant type 7, autosomal dominant non-syndromic intellectual disability 7, intellectual disability, autosomal dominant 7, mental retardation, autosomal dominant 7
0 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Broader categories
Disease
(717)
Nervous system disorder
(243)
Hereditary disease
(188)
Neurodevelopmental disorder
(154)
Intellectual disability
(133)
Syndromic disease
(25)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Hereditary neurological disease
(6)
Disease of genetic or genomic mechanism
(2)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.